All pharma Events (60)

September 15Monday

GMP Compliance for Pharmaceutical Quality Control Laboratories: 2-day In-person Seminar

September 15, 2014 at 9am to September 16, 2014 at 6pm – w hong kong Overview: This course is designed for people who are growing in their knowledge of pharmaceutical quality control practices and regulations. It will be a "how to" course where the instructor will exp… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda

October 23Thursday

2-day In-person Seminar on “Quality System Regulations for Drugs, Devices, and Tablets and How to generate your DMF” at Philadelphia

October 23, 2014 at 9am to October 24, 2014 at 6pm – Philadelphia, PA Detailed Description: Primary Student Objectives - General High Level Topics where we will move down to very specific discussion and details to generate a much higher comprehension for quality indivi… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
2-day In-person Seminar on “Applying ISO14971:2012 and IEC62304 - A Guide to Practical Risk Management” in Berlin, Germany

October 23, 2014 at 9am to October 24, 2014 at 6pm – Berlin, Germany Summary of the Workshop: Gaps, incorrect or incomplete implementation of safety functionality can delay or make the certification/approval of medical products impossible. Most activities cannot be re… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda

October 30Thursday

2-day In-person Seminar on “The A to Z's of HIPAA Privacy, Security, and Breach Notification Rules” at Raleigh, NC

October 30, 2014 at 9am to October 31, 2014 at 6pm – Raleigh, NC Summary of the workshop: This session is designed to provide intensive, two-day training in HIPAA compliance, including what's new in the regulations, what's changed recently, and what needs to be ad… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
2-day In-person Seminar on “Combination Products: How to Get Your Combination Product Approved and onto the US Marketplace” at San Francisco

October 30, 2014 at 9am to October 31, 2014 at 6pm – San Francisco, CA, USA Summary of the workshop: This course provides a comprehensive understanding of the FDA Combination Product system. Participants receive a foundation of knowledge about the FDA Office of Combination P… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda
2-day In-person Seminar on “Quality Audits for the Medical Device Industry” at Raleigh, NC

October 30, 2014 at 9am to October 31, 2014 at 6pm – Raleigh, NC Summary of the workshop: Quality audits are an important element in checking the health of a Quality Management System (QMS). Audits are one of the most powerful tools that management has to assure o… Organized by GlobalCompliancePanel | Type: seminar, pharma, medical, clinical, health, compliance, regulatory, fda

February 4Thursday

Seminar on Modern Approaches to Process Validation: Requirements for Process Design, Design of Facilities and the Qualification of Equipment and Utilities at Mumbai

February 4, 2016 at 9am to February 5, 2016 at 6pm – The LaLiT Mumbai Overview: Companies face many common issues and confusion when creating or revamping their validation programs. Some of these common issues are: Company has expertise in its process validation progr… Organized by John Robinson | Type: seminar, pharma, medical, process, validation

April 28Thursday

Seminar on Validation and Part 11 Compliance of Computer Systems and Data at Mumbai

April 28, 2016 at 9am to April 29, 2016 at 6pm – The LaLiT Mumbai Overview: This 2-day course provides the regulatory background and guides attendees through the complete equipment qualification, calibration and computer system validation processes from planning to… Organized by John Robinson | Type: seminar, pharma, medical, fda, validation, complaince

December 3Thursday

The Risk-Based Approach to Pharmacovigilance Audits - A Practical Approach to Design and Implementation

December 3, 2020 at 8am to December 4, 2020 at 4pm – online The European Medicines Agency's (EMA) Guideline on good pharmacovigilance practices (GVP), Module IV requires that risk-based audits of the quality system be performed at regular intervals to assure… Organized by ComplianceOnline | Type: pharma

February 22Tuesday

Structuring and Conducting Risk-Based Internal cGMP Compliance Audits

February 22, 2022 from 10am to 1pm – online This training will evaluate the chief areas of an FDA cGMP compliance audit and help you understand the actual and anticipated changes in emphasis based on this new regulatory climate. It will prepar… Organized by ComplianceOnline | Type: pharma